# FDA Inspection 792958 - Sunnex, LLC - July 30, 2012

Source: https://www.keypedia.com/records/fda_inspections/sunnex-llc/6c1444bf-55ac-4f32-a3c5-d0c84bc50f4f
Source feed: FDA_Inspections

> FDA Inspection 792958 for Sunnex, LLC on July 30, 2012. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 792958
- Company Name: Sunnex, LLC
- Inspection Date: 2012-07-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1162566 - 2022-02-18](https://www.keypedia.com/records/fda_inspections/sunnex-llc/0e286b75-18dd-45fe-84c4-10223d7cf290)
- [FDA Inspection 1162566 - 2022-02-18](https://www.keypedia.com/records/fda_inspections/sunnex-llc/877774ee-b226-4c76-b172-2cbb13924eb8)
- [FDA Inspection 1095148 - 2019-07-03](https://www.keypedia.com/records/fda_inspections/sunnex-llc/26a0ffe4-54b4-4775-9c36-1a9ee275590f)
- [FDA Inspection 1095148 - 2019-07-03](https://www.keypedia.com/records/fda_inspections/sunnex-llc/812548dd-e6fa-48c3-b7e5-2f3dbdea4595)
- [FDA Inspection 1017642 - 2017-07-12](https://www.keypedia.com/records/fda_inspections/sunnex-llc/86fe1ccc-24db-44fb-bde4-82a285dc77e1)

Company: https://www.keypedia.com/companies/sunnex-llc/8a909b31-6bcb-4a15-9c5e-c1f91bb4f858

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7